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Center for Clinical Imaging Research (CCIR)

Before participating in a research study, you must review and sign an Informed Consent Form. This form will provide detailed information about why the study is being conducted, what you will be asked to do for the study, a description of the study procedures, an explanation of the costs, risks, benefits, confidentiality issues, as well as, other details related to your participation. A member of the research staff will go over the Consent Form with you in detail before you are asked to sign it and become a participant in the study.